Developmental pharmacology—drug disposition, action, and therapy in infants and children
GL Kearns, SM Abdel-Rahman… - … England Journal of …, 2003 - Mass Medical Soc
For those using drugs to treat infants and children, the integration of developmental
pharmacology is crucial to appropriate clinical practice. Changes in metabolic capacity …
pharmacology is crucial to appropriate clinical practice. Changes in metabolic capacity …
Ontogeny of drug metabolizing enzymes in the neonate
Fetal exposure to xenobiotics is modulated to a considerable degree by the metabolic
capabilities of the mother and the placenta. However, once liberated from the uterine …
capabilities of the mother and the placenta. However, once liberated from the uterine …
[图书][B] Handbook of toxicology
MJ Derelanko, MA Hollinger - 2001 - api.taylorfrancis.com
LOCATE FREQUENTLY USED INFORMATION EASILY AND QUICKLYWorking in the
laboratory or office, you use a diverse assortment of basic information to design, conduct …
laboratory or office, you use a diverse assortment of basic information to design, conduct …
Differences in absorption, distribution, metabolism and excretion of xenobiotics between the paediatric and adult populations
M Strolin Benedetti, R Whomsley… - Expert opinion on drug …, 2005 - Taylor & Francis
In children, the therapeutic benefits and potential risks associated with drug treatment may
be different from those in adults and will depend on the exposure, receptor sensitivity and …
be different from those in adults and will depend on the exposure, receptor sensitivity and …
Drug labeling and exposure in neonates
MM Laughon, D Avant, N Tripathi, CP Hornik… - JAMA …, 2014 - jamanetwork.com
Importance Federal legislation has led to a notable increase in pediatric studies submitted to
the Food and Drug Administration (FDA), resulting in new pediatric information in product …
the Food and Drug Administration (FDA), resulting in new pediatric information in product …
Impact of developmental pharmacology on pediatric study design: overcoming the challenges
GL Kearns - Journal of allergy and clinical immunology, 2000 - Elsevier
The need to establish drug-dosing guidelines in children highlights the challenges
associated with the development of phases I and II pediatric clinical trials. These challenges …
associated with the development of phases I and II pediatric clinical trials. These challenges …
Developmental pharmacokinetics
JN van den Anker, M Schwab, GL Kearns - Pediatric clinical pharmacology, 2011 - Springer
The advances in developmental pharmacokinetics during the past decade reside with an
enhanced understanding of the influence of growth and development on drug absorption …
enhanced understanding of the influence of growth and development on drug absorption …
[HTML][HTML] Assessment of age-related changes in pediatric gastrointestinal solubility
Purpose Compound solubility serves as a surrogate indicator of oral biopharmaceutical
performance. Between infancy and adulthood, marked compositional changes in …
performance. Between infancy and adulthood, marked compositional changes in …
Nanomedicines in the future of pediatric therapy
A Sosnik, AM Carcaboso - Advanced Drug Delivery Reviews, 2014 - Elsevier
Nanotechnology has become a key tool to overcome the main (bio) pharmaceutical
drawbacks of drugs and to enable their passive or active targeting to specific cells and …
drawbacks of drugs and to enable their passive or active targeting to specific cells and …
Famotidine for infant gastrooesophageal reflux: a multicentre, randomized, placebocontrolled, withdrawal trial
SR Orenstein, TM Shalaby… - Alimentary …, 2003 - Wiley Online Library
Background: Gastrooesophageal reflux afflicts up to 7% of all infants. Histamine2 receptor
antagonists are the most commonly prescribed medications for this disorder, but few …
antagonists are the most commonly prescribed medications for this disorder, but few …